Incidental Mutation 'IGL02977:Or5d37'
| ID |
406429 |
| Institutional Source |
Australian Phenomics Network
(link to record)
|
| Gene Symbol |
Or5d37
|
| Ensembl Gene |
ENSMUSG00000075136 |
| Gene Name |
olfactory receptor family 5 subfamily D member 37 |
| Synonyms |
GA_x6K02T2Q125-49585842-49584862, Olfr1164, MOR174-11 |
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.096)
|
| Stock # |
IGL02977
|
| Quality Score |
|
|
Status
|
|
| Chromosome |
2 |
| Chromosomal Location |
87923199-87924310 bp(-) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
T to C
at 87923915 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Isoleucine to Valine
at position 122
(I122V)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000097422
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000099834]
|
| AlphaFold |
A2AVT5 |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000099834
AA Change: I122V
PolyPhen 2
Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
|
| SMART Domains |
Protein: ENSMUSP00000097422
Gene: ENSMUSG00000075136
AA Change: I122V
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:7tm_4
|
43 |
320 |
3.8e-47 |
PFAM |
|
Pfam:7tm_1
|
53 |
302 |
2.9e-15 |
PFAM |
|
| Coding Region Coverage |
|
| Validation Efficiency |
|
| MGI Phenotype |
FUNCTION: Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 32 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 2810004N23Rik |
C |
T |
8: 125,587,930 (GRCm39) |
V57M |
probably benign |
Het |
| 4933440M02Rik |
T |
A |
7: 124,930,874 (GRCm39) |
|
noncoding transcript |
Het |
| Bmp5 |
A |
G |
9: 75,801,081 (GRCm39) |
T404A |
probably damaging |
Het |
| Cep192 |
T |
C |
18: 67,985,976 (GRCm39) |
V1660A |
probably damaging |
Het |
| Csmd2 |
C |
A |
4: 128,387,069 (GRCm39) |
Y2121* |
probably null |
Het |
| Daam1 |
G |
A |
12: 71,990,946 (GRCm39) |
A187T |
unknown |
Het |
| Dnaja4 |
T |
C |
9: 54,621,794 (GRCm39) |
L343P |
possibly damaging |
Het |
| Dym |
T |
C |
18: 75,196,246 (GRCm39) |
|
probably null |
Het |
| F5 |
A |
T |
1: 164,021,590 (GRCm39) |
D1355V |
probably damaging |
Het |
| Fcgbpl1 |
C |
T |
7: 27,863,797 (GRCm39) |
T2523M |
possibly damaging |
Het |
| Gcnt1 |
A |
T |
19: 17,306,738 (GRCm39) |
I329N |
probably damaging |
Het |
| Gm10110 |
T |
C |
14: 90,134,768 (GRCm39) |
|
noncoding transcript |
Het |
| Hdgfl2 |
A |
G |
17: 56,406,319 (GRCm39) |
N569S |
possibly damaging |
Het |
| Hivep1 |
T |
C |
13: 42,309,412 (GRCm39) |
S551P |
possibly damaging |
Het |
| Hpse2 |
G |
A |
19: 42,777,561 (GRCm39) |
|
probably benign |
Het |
| Hspe1 |
T |
C |
1: 55,130,232 (GRCm39) |
Y88H |
probably benign |
Het |
| Ifi44 |
A |
T |
3: 151,445,016 (GRCm39) |
M312K |
probably benign |
Het |
| Lrp1b |
T |
G |
2: 40,620,747 (GRCm39) |
D3577A |
probably damaging |
Het |
| Mapk13 |
G |
T |
17: 28,995,322 (GRCm39) |
G181V |
probably damaging |
Het |
| Oprl1 |
G |
T |
2: 181,360,304 (GRCm39) |
C115F |
probably damaging |
Het |
| Or4d1 |
A |
G |
11: 87,804,956 (GRCm39) |
S259P |
possibly damaging |
Het |
| Psg22 |
A |
G |
7: 18,453,524 (GRCm39) |
D112G |
probably benign |
Het |
| Rp1l1 |
T |
A |
14: 64,265,599 (GRCm39) |
I395N |
probably benign |
Het |
| Simc1 |
T |
C |
13: 54,674,120 (GRCm39) |
S823P |
probably benign |
Het |
| Slc9b1 |
T |
C |
3: 135,103,484 (GRCm39) |
L538P |
probably damaging |
Het |
| Smad2 |
T |
A |
18: 76,422,235 (GRCm39) |
Y216N |
possibly damaging |
Het |
| Stxbp2 |
A |
T |
8: 3,691,971 (GRCm39) |
I538F |
probably benign |
Het |
| Tonsl |
T |
A |
15: 76,517,073 (GRCm39) |
Q882L |
probably benign |
Het |
| Trav13-2 |
C |
T |
14: 53,872,764 (GRCm39) |
T80I |
probably damaging |
Het |
| Uaca |
C |
T |
9: 60,773,662 (GRCm39) |
P388S |
probably benign |
Het |
| Vmn2r116 |
A |
G |
17: 23,607,748 (GRCm39) |
R439G |
possibly damaging |
Het |
| Vmn2r18 |
C |
A |
5: 151,510,149 (GRCm39) |
A75S |
probably damaging |
Het |
|
| Other mutations in Or5d37 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL01522:Or5d37
|
APN |
2 |
87,923,360 (GRCm39) |
missense |
possibly damaging |
0.48 |
|
IGL02894:Or5d37
|
APN |
2 |
87,924,107 (GRCm39) |
missense |
possibly damaging |
0.79 |
|
R0234:Or5d37
|
UTSW |
2 |
87,923,366 (GRCm39) |
nonsense |
probably null |
|
|
R0234:Or5d37
|
UTSW |
2 |
87,923,366 (GRCm39) |
nonsense |
probably null |
|
|
R0480:Or5d37
|
UTSW |
2 |
87,923,972 (GRCm39) |
missense |
probably benign |
|
|
R0644:Or5d37
|
UTSW |
2 |
87,923,633 (GRCm39) |
missense |
probably benign |
0.02 |
|
R1479:Or5d37
|
UTSW |
2 |
87,923,630 (GRCm39) |
missense |
probably benign |
0.05 |
|
R2047:Or5d37
|
UTSW |
2 |
87,924,237 (GRCm39) |
missense |
probably benign |
0.01 |
|
R2311:Or5d37
|
UTSW |
2 |
87,924,178 (GRCm39) |
missense |
probably benign |
0.00 |
|
R2973:Or5d37
|
UTSW |
2 |
87,923,458 (GRCm39) |
missense |
probably benign |
0.00 |
|
R3683:Or5d37
|
UTSW |
2 |
87,923,603 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R3685:Or5d37
|
UTSW |
2 |
87,923,603 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4258:Or5d37
|
UTSW |
2 |
87,923,362 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4811:Or5d37
|
UTSW |
2 |
87,923,876 (GRCm39) |
missense |
probably benign |
0.08 |
|
R4970:Or5d37
|
UTSW |
2 |
87,923,353 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5112:Or5d37
|
UTSW |
2 |
87,923,353 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5258:Or5d37
|
UTSW |
2 |
87,923,762 (GRCm39) |
missense |
probably benign |
0.22 |
|
R5884:Or5d37
|
UTSW |
2 |
87,924,140 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6329:Or5d37
|
UTSW |
2 |
87,924,008 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6597:Or5d37
|
UTSW |
2 |
87,923,413 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7018:Or5d37
|
UTSW |
2 |
87,923,600 (GRCm39) |
missense |
probably benign |
0.00 |
|
R7055:Or5d37
|
UTSW |
2 |
87,924,045 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7314:Or5d37
|
UTSW |
2 |
87,923,458 (GRCm39) |
missense |
probably benign |
0.00 |
|
R7350:Or5d37
|
UTSW |
2 |
87,923,542 (GRCm39) |
missense |
probably benign |
0.01 |
|
R7527:Or5d37
|
UTSW |
2 |
87,923,954 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8003:Or5d37
|
UTSW |
2 |
87,923,589 (GRCm39) |
nonsense |
probably null |
|
|
R8814:Or5d37
|
UTSW |
2 |
87,923,315 (GRCm39) |
missense |
probably benign |
|
|
R9072:Or5d37
|
UTSW |
2 |
87,924,172 (GRCm39) |
missense |
probably benign |
0.25 |
|
R9073:Or5d37
|
UTSW |
2 |
87,924,172 (GRCm39) |
missense |
probably benign |
0.25 |
|
R9189:Or5d37
|
UTSW |
2 |
87,924,194 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9276:Or5d37
|
UTSW |
2 |
87,923,806 (GRCm39) |
missense |
probably benign |
|
|
R9284:Or5d37
|
UTSW |
2 |
87,924,278 (GRCm39) |
start codon destroyed |
probably benign |
|
|
Z1176:Or5d37
|
UTSW |
2 |
87,923,678 (GRCm39) |
missense |
probably damaging |
0.99 |
|
| Posted On |
2016-08-02 |
Incidental Mutation